USING TREND INDICES FOR ENDANGERED SPECIES

Initial appraisals of the status of endangered large-mammal populations may have to depend on indices of population trend. Such indices may possibly be improved by using auxiliary variables. Various models were studied for populations of the Florida manatee (Trichechus manatus latirostris), Yellowstone grizzly bear (Ursus arctos horribilis), and Hawaiian monk seal (Monachus schauinslandi). Several criteria for checking validity of the fitted models were considered, and the simple R² criterion appears to provide useful comparisons. Multiple regression models overestimated the rate of change of the East Coast manatee population as determined from three other sources (a covariance model, a non-linear model, and the rate estimated from reproductive and survival data). A multiple regression model for grizzly bears using three auxiliary variables exhibited a fairly high R² (0.84) and appeared to provide a better fit than did a non-linear model. A beach count index for Hawaiian monk seals seemed to be unreliable for year-to-year comparisons in contrast to total population counts and estimates from a capture-recapture method. The use of auxiliary variables for checking and improving trend index data appears feasible and well worthwhile.     

Grizzly bear population vital rates and trend in the Northern Continental Divide Ecosystem,Montana

We estimated grizzly bear (Ursus arctos) population vital rates and trend for the Northern Continental Divide Ecosystem (NCDE), Montana, between 2004 and 2009 by following radio-collared females and observing their fate and reproductive performance. Our estimates of dependent cub and yearling survival were 0.612 (95% CI = 0.300–0.818) and 0.682 (95% CI = 0.258–0.898). Our estimates of subadult and adult female survival were 0.852 (95% CI = 0.628–0.951) and 0.952 (95% CI = 0.892–0.980). From visual observations, we estimated a mean litter size of 2.00 cubs/litter. Accounting for cub mortality prior to the first observations of litters in spring, our adjusted mean litter size was 2.27 cubs/litter. We estimated the probabilities of females transitioning from one reproductive state to another between years. Using the stable state probability of 0.322 (95% CI = 0.262–0.382) for females with cub litters, our adjusted fecundity estimate (m_x) was 0.367 (95% CI = 0.273–0.461). Using our derived rates, we estimated that the population grew at a mean annual rate of approximately 3% (λ = 1.0306, 95% CI = 0.928–1.102), and 71.5% of 10,000 Monte Carlo simulations produced estimates of λ > 1.0. Our results indicate an increasing population trend of grizzly bears in the NCDE. Coupled with concurrent studies of population size, we estimate that over 1,000 grizzly bears reside in and adjacent to this recovery area. We suggest that monitoring of population trend and other vital rates using radioed females be continued. © 2011 The Wildlife Society.     

Intraspecific Variation in Home Range Overlap with Habitat Quality: A Comparison among Brown Bear Populations

We developed a conceptual model of spatial organization in vertebrates based upon changes in home range overlap with habitat quality. We tested the model using estimates of annual home ranges of adult females and densities for 30 populations of brown bears (Ursus arctos) in North America. We used seasonality as a surrogate of habitat quality, measured as the coefficient of variation among monthly actual evapotranspiration values for areas in which study populations were located. We calculated home range overlap for each population as the product of the average home range size for adult females and the estimated population density of adult females. Home range size varied positively with seasonality; however, home range overlap varied with seasonality in a nonlinear manner. Areas of low and high seasonality supported brown bears with considerable home range overlap, but areas of moderate seasonality supported brown bears with low home range overlap. These results are consistent with behavioural theory predicting a nonlinear relationship between food availability and territoriality.     

Effect of Harvest on a Brown Bear Population in Alaska

There is a long and contentious history of brown bear (Ursus arctos) harvest management in Alaska, USA, the state that hosts the largest brown bear population in North America. In the mid-1990s, the Alaska Board of Game set the population objective for brown bears in Game Management Unit 13 A, located in interior southcentral Alaska, to be reduced by 50% to improve survival of moose (Alces alces) calves. The Board began further liberalizing brown bear harvest regulations for the unit beginning in regulatory year 1995, though adult females and their dependent offspring (i.e., cubs <2 yrs old) were protected. To evaluate progress toward this abundance objective, we captured and collared bears between 2006 and 2011 and conducted a capture-mark-resight density survey during summer 2011 for comparison to a similar baseline survey conducted in 1998. We report the results of the density survey and vital rates estimated from resight histories of collared bears and harvest information spanning from 1985 (10 years before establishment of the population objective) to 2012. There was a 25–40% reduction in abundance between 1998 and 2011. Population growth rates derived from density estimates and a matrix population projection model indicated that the population declined by 2.3–4.2% annually. We estimated harvest rates to be 8–15% annually, but harvest composition data indicated no changes in skull size, age distribution, or overall sex ratio. There was evidence of an increase in the proportion of older females in the harvest. Demographic analysis indicated high reproductive output and recruitment, potentially indicating a density-dependent compensatory response to reduced population size. Despite 13 years of harvest rates in excess of what had previously been considered to be sustainable for this population, the objective of reducing bear abundance by 50% had not been achieved as of 2011. The protection of females and dependent offspring in our study population appears to be a sufficient safeguard against a precipitous population decline while still permitting progress toward the population objective through high harvest on other segments of the population. © 2020 The Wildlife Society.     

Woodland caribou calf mortality in Newfoundland: insights into the role of climate,predation and population density over three decades of study

The rates and causes of juvenile mortality are central features of the dynamics and conservation of large mammals, like woodland caribou (Rangifer tarandus caribou (Gmelin, 1788)), but intrinsic and extrinsic factors may be modified by variations in animal abundance. We tested the influences of population size, climate, calf weight and sex on survival to 6 months of age of 1241 radio-collared caribou calves over three decades, spanning periods of population growth (1979–1997) and decline (2003–2012) in Newfoundland, Canada. Daily survival rates were higher and rose more quickly with calf age during the population growth period compared to the decline. Population size (negatively) and calf weight (positively) affected survival during the decline but neither had a detectable influence during the growth phase. Sex, climate and plant productivity (the latter two derived from the North Atlantic Oscillation and Normalized Difference Vegetation Index, respectively) exerted minimal influence during either phase. Predation was the dominant source of mortality. The mean percentage of calves killed by predators was 30 % higher during the decline compared to the growth phase. Black bears (Ursus americanus) and lynx (Lynx canadensis) were the major predators during the population increase but this changed during the decrease to black bears and coyotes (Canis latrans). Our findings are consistent with the hypothesis that Newfoundland caribou experienced phase-dependent survival mediated proximally by predation and competition for food.     

Integrating distance sampling survey data with population indices to separate trends in abundance and temporary immigration

Managers rely on accurate estimators of wildlife abundance and trends for management decisions. Despite the focus of contemporary wildlife science on developing methods to improve inference from wildlife surveys, legacy datasets often rely on index counts that lack information about the detection process. Data integration can be a useful tool for combining index counts with data collected under more rigorous designs (i.e., designs that account for the detection process), but care is required when datasets represent different population processes or are mismatched in space and time. This can be particularly problematic in cases where animals aggregate in response to a spatially or temporally limited resource because individuals may temporarily immigrate from outside the study area and be included in the abundance index. Abundance indices based on brown bear (Ursus arctos) feeding aggregations within coastal meadows in early summer in Lake Clark National Park and Preserve, Alaska, USA, are one such example. These indices reflect the target population (brown bears residing within the park) and temporary immigrants (i.e., bears drawn from outside the park boundary). To properly account for the effects of temporary immigration, we integrated the index data with abundance data collected via park-wide distance sampling surveys, the latter of which properly addressed the detection process. By assuming that the distance data provide inference on abundance and the index counts represent some combination of abundance and temporary immigration processes, we were able to decompose the relative contribution of each to overall trend. We estimated that the density of brown bears within our study area was 38–54 adults/1,000 km² during 2003–2019 and that abundance increased at a rate of approximately 1.4%/year. The contribution of temporary immigrants to overall trend in the index was low, so we created 3 hypothetical scenarios to more fully demonstrate how the integrated approach could be useful in situations where the composite trend in meadow counts may obscure trends in abundance (e.g., opposing trends in abundance and temporary immigration). Our work represents a conceptual advance supporting the integration of legacy index data with more rigorous data streams and is broadly applicable in cases where trends in index values may represent a mixture of population processes.     

Evidence for density-dependent effects on body composition of a large omnivore in a changing Greater Yellowstone Ecosystem

Understanding the density-dependent processes that drive population demography in a changing world is critical in ecology, yet measuring performance–density relationships in long-lived mammalian species demands long-term data, limiting scientists' ability to observe such mechanisms. We tested performance–density relationships for an opportunistic omnivore, grizzly bears (Ursus arctos, Linnaeus, 1758) in the Greater Yellowstone Ecosystem, with estimates of body composition (lean body mass and percent body fat) serving as indicators of individual performance over two decades (2000–2020) during which time pronounced environmental changes have occurred. Several high-calorie foods for grizzly bears have mostly declined in recent decades (e.g., whitebark pine [Pinus albicaulis, Engelm, 1863]), while increasing human impacts from recreation, development, and long-term shifts in temperatures and precipitation are altering the ecosystem. We hypothesized that individual lean body mass declines as population density increases (H1), and that this effect would be more pronounced among growing individuals (H2). We also hypothesized that omnivory helps grizzly bears buffer energy intake from changing foods, with body fat levels being independent from population density and environmental changes (H3). Our analyses showed that individual lean body mass was negatively related to population density, particularly among growing-age females, supporting H1 and partially H2. In contrast, population density or sex had little effect on body fat levels and rate of accumulation, indicating that sufficient food resources were available on the landscape to accommodate successful use of shifting food sources, supporting H3. Our results offer important insights into ecological feedback mechanisms driving individual performances within a population undergoing demographic and ecosystem-level changes. However, synergistic effects of continued climate change and increased human impacts could lead to more extreme changes in food availability and affect observed population resilience mechanisms. Our findings underscore the importance of long-term studies in protected areas when investigating complex ecological relationships in an increasingly anthropogenic world.     

Feeding habits may explain the morphological uniqueness of brown bears on Etorofu Island,Southern Kuril Islands in East Asia

The brown bear (Ursus arctos) population on Etorofu Island, Southern Kuril Islands, has several unique morphological features: (1) the presence of white‐pelage bears within the population and (2) a larger body size than bears on a larger neighbour island, Hokkaido Island. Nevertheless, little ecological information is available about Etorofu brown bears. In the present study, we reveal the unique feeding habits of Etorofu brown bears and suggest that their unique morphological features and diet are related. The feeding habits of brown bears on Etorofu Island were assessed using carbon, nitrogen, and sulfur stable isotope analysis, and their feeding habits were compared with those of bears on the eastern side of Hokkaido Island. According to the stable isotope analysis, the dependence on salmon is great for bears on Etorofu but only slight for bears on Hokkaido. Our results suggest that the feeding habits of Etorofu brown bears may explain their unique morphological features because a white pelage colour confers an advantage when catching salmon, and a carnivorous diet can make their body size larger. The variation in feeding habits can be an important driver of the speciation and evolution of animals.     

Bear historical ranges revisited: Documenting the increase of a once-extirpated population in Nevada

Black bears (Ursus americanus) were once abundant in Nevada and distributed throughout the state, yet recognition of the species' historical occurrence in the state is uncommon and has therefore been ignored in published distribution maps for North America. The lack of representation on distribution maps is likely due to the lack of any scientific data or research on bears in Nevada until 1987. Historical records dating back to the 1840s compiled by Nevada Department of Wildlife (NDOW) biologist Robert McQuivey indicate presence of black bears throughout the state in the 1800s through about 1930. The paucity of historical references after 1931 suggest extirpation of black bears from Nevada's interior mountain ranges by this time. We report on historical records of black bears in the state of Nevada and the results of a current population estimate of black bears derived from a sample of marked bears (n = 420) captured 707 times between 1997 and 2008. Using Pradel and Cormack–Jolly–Seber models in Program MARK, we estimated overall population size, finite rate of growth (λ = 1.16), quarterly and annual survival rates for males and females, seasonal capture probabilities, and recruitment rates. Our results indicate an overall population size of 262 ± 31 adult black bears in western Nevada. These results suggest that the once abundant, then extirpated population of black bears in Nevada is increasing at an annual average rate of 16%. Although the current distribution is limited to the western part of the state, our findings suggest possible expansion of the population into historical habitat within the interior and eastern portions of the state that have been absent of bears for >80 years. Finally, based on historical records, we present suggested revised historical distribution maps for black bears that include the Great Basin ranges in Nevada. © 2013 The Wildlife Society.     

Demography of Black Bears in Hunted and Unhunted Areas of the Boreal Forest of Ontario

Abstract: We estimated relative density, survival, and reproduction of American black bears (Ursus americanus) from capture-recapture and telemetry data collected from 1989 to 1999 in the unhunted Chapleau Crown Game Preserve (CCGP) and nearby hunted areas in the boreal forest of Ontario, Canada. We tested for combinations of effects of age class, sex, year, years of food shortage, encumbrance status, and residency (on or off the Game Preserve) on vital rates. Results from live captures, remote captures, and bait-station hit rates indicated that density was highest inside CCGP. Total survival of adult females, subadults, and cubs were similar among residents and nonresidents of CCGP, but yearling survival was lower among CCGP residents. Adult females were approximately twice as likely to die and nearly 10 times as likely to be cannibalized (risk ratio [RR] = 9.62, 95% CI = 2.088–44.29) while encumbered with cubs of the year. Nonresidents of CCGP had greater risk of being harvested (RR = 4.00, 95% CI = 1.19–13.46) but similar risk of being cannibalized (RR = 0.875, 95% CI = 0.300–2.55) relative to CCGP residents, suggesting that harvest mortality was additive to other forms of mortality. Residents of CCGP had older ages at primiparity and lower litter-production rates than bears resident in hunted areas. Few litters were produced in years following food shortages, but litter size was unaffected. We recommend that managers allow for additive harvest mortality and reduced survival of bears encumbered with cubs of the year, and we caution that assuming density-compensatory increases in cub production could optimistically bias estimates of population growth.     

Influence of whitebark pine decline on fall habitat use and movements of grizzly bears in the Greater Yellowstone Ecosystem

When abundant, seeds of the high‐elevation whitebark pine (WBP; Pinus albicaulis) are an important fall food for grizzly bears (Ursus arctos) in the Greater Yellowstone Ecosystem. Rates of bear mortality and bear/human conflicts have been inversely associated with WBP productivity. Recently, mountain pine beetles (Dendroctonus ponderosae) have killed many cone‐producing WBP trees. We used fall (15 August–30 September) Global Positioning System locations from 89 bear years to investigate temporal changes in habitat use and movements during 2000–2011. We calculated Manly–Chesson (MC) indices for selectivity of WBP habitat and secure habitat (≥500 m from roads and human developments), determined dates of WBP use, and documented net daily movement distances and activity radii. To evaluate temporal trends, we used regression, model selection, and candidate model sets consisting of annual WBP production, sex, and year. One‐third of sampled grizzly bears had fall ranges with little or no mapped WBP habitat. Most other bears (72%) had a MC index above 0.5, indicating selection for WBP habitats. From 2000 to 2011, mean MC index decreased and median date of WBP use shifted about 1 week later. We detected no trends in movement indices over time. Outside of national parks, there was no correlation between the MC indices for WBP habitat and secure habitat, and most bears (78%) selected for secure habitat. Nonetheless, mean MC index for secure habitat decreased over the study period during years of good WBP productivity. The wide diet breadth and foraging plasticity of grizzly bears likely allowed them to adjust to declining WBP. Bears reduced use of WBP stands without increasing movement rates, suggesting they obtained alternative fall foods within their local surroundings. However, the reduction in mortality risk historically associated with use of secure, high‐elevation WBP habitat may be diminishing for bears residing in multiple‐use areas.     

Components of Grizzly Bear Habitat Selection: Density,Habitats, Roads,and Mortality Risk

Abstract: We used resource selection functions (RSF) to estimate the relative probability of use for grizzly bears (Ursus arctos) adjacent to the Parsnip River, British Columbia, Canada, 1998-2003. We collected data from 30 radiocollared bears on a rolling plateau where a large portion of the landscape had been modified by human activities, primarily forestry. We also monitored 24 radiocollared bears in mountain areas largely inaccessible to humans. Bears that lived on the plateau existed at less than one-quarter the density of bears in the mountains. Plateau bears ate more high-quality food items, such as meat and berries, leading us to conclude that food limitation was not responsible for the differences in densities. We hypothesized that plateau bears were limited by human-caused mortality associated with roads constructed for forestry activities. Independent estimates of bear population size from DNA-based mark-recapture techniques allowed us to link populations to habitats using RSF models to scale habitat use patterns to population density. To evaluate whether differences in land-cover type, roads, or mortality risk could account for the disparity in density we used the mountain RSF model to predict habitat use and number of bears on the plateau and vice versa. We predicted increases ranging from 34 bears to 96 bears on the plateau when switching model coefficients, excluding land-cover types; when exchanging land-cover coefficients, the model predicted that the plateau population would be 9 bears lower than was observed. Large reductions in the numbers of mountain bears were predicted by habitat-selection models of bears using the plateau landscape. Although RSF models estimated in mountain and plateau landscapes could not predict bear use and abundance in the other areas, contrasts in models between areas provided a useful tool for examining the effects of human activities on grizzly bears.     

2-Aminoanthracene, diethylstilboestrol and vinblastine tested in the in vitro mammalian cell micronucleus test at British American Tobacco UK in support of the OECD draft Test Guideline 487

Reference genotoxic compounds 2-aminoanthracene, diethylstilboestrol and vinblastine were tested in the in vitro micronucleus assay using Chinese hamster V79 derived cells in the laboratories of British American Tobacco in the UK. The work was conducted in support of the cytotoxicity measures recommended in the 2007 version of the OECD Test Guideline 487. The three compounds were positive in the assay in the presence and absence of the cytokinesis blocking agent cytochalasin B at concentrations that did not exceed the recommended cytotoxic limits determined by relative population doubling, relative increase in cell counts, relative cell counts and cytokinesis block proliferation index. Consequently, this work supports the hypothesis that relative population doubling, relative increase in cell counts and relative cell counts are appropriate measures of cytotoxicity for the non-cytokinesis blocked in vitro micronucleus assay.     

Relationship Between Fecal Pellet Counts and Snowshoe Hare Density in Western Wyoming

ABSTRACT Snowshoe hares (Lepus americanus) are an important prey species for Canada lynx (Lynx canadensis) and are considered critical for lynx population persistence. Determination of snowshoe hare distribution and abundance is needed by land management agencies for lynx conservation. An accepted approach for estimating snowshoe hare abundance is the use of fecal-pellet plot counts. Locally derived regression equations are preferred for accurate calibration of pellet counts to snowshoe hare density due to local differences in pellet deposition and decomposition. We used linear regression to examine correlations between snowshoe hare density, as determined by mark–recapture estimates, and pellet plot counts on both uncleared plots and annually cleared plots on the Bridger-Teton National Forest, western Wyoming, USA. We found significant correlations between snowshoe hare density estimates and fecal pellet counts for both uncleared and annually cleared pellet counts; however, the relationship was stronger (higher r) when using pellet counts from annually cleared plots. In addition, we found that adjusting the buffer size by omitting hard habitat edges (not used by hares) around trapping grids improved correlations between snowshoe hare density and fecal pellet counts for both uncleared plots and annually cleared plots. Though precision is sacrificed when using uncleared plots, they may be useful as a coarse index of habitat use by snowshoe hares. Our derived regression equations may be useful to identify important foraging habitat for Canada lynx in western Wyoming. Land managers responsible for conserving snowshoe hare habitat in western Wyoming may use these equations to monitor changes in hare populations among habitats and during prescribed management actions.     

Expansion of Brown Bears (Ursus arctos) into the Eastern Alps: A Spatially Explicit Population Model

We present a spatially explicit population model for analysing the expansion of brown bears (Ursus arctos) after the reintroduction program in central Austria. The model is based on field investigations into brown bears in Austria and Slovenia and on current knowledge of brown bears. The landscape of the eastern Alps is represented by a GIS-derived raster map defining local habitat suitability and five major spatial barriers to dispersal. The population model follows the fate of individual bears and simulates reproduction, dispersal, home range establishment, and mortality in annual time steps. We indirectly adjust unknown or uncertain model parameters with 10-year data on the number of females with cubs in central Austria and determine key variables of population dynamics, such as population sizes and growth rates within different population nuclei, dispersal distances, or mortality rates, for model parameterisations that reproduce the data on females with cubs. We estimated a current (1996–2000) growth rate of the population in Austria and adjacent parts of Italy of some 14%; a high proportion of this growth was due toimmigration from Slovenia. Consequently, the growth rate of the subpopulation in central Austria, which probably is isolated functionally (i.e., no exchange of females) from the nuclei along the Austrian–Slovenian border, yielded some 7%. This subpopulation may comprise seven residents, and we estimated for females a 33% risk of extinction during the 1992–2000 period. Validation and confirmation of our model results with data on bear densities that were not used for model construction and parameterisation supported our findings. The high female mortality rates, together with the vulnerability of the small population to chance events (i.e., demographic stochasticity), are the most pressing threat for the population in the eastern Alps. Our approach could be widely applied for analysing dynamics of rare and endangered species in which the paucity of data precludes an appraisal of the state of the population using standard methods.     

Mark–recapture using tetracycline and genetics reveal record-high bear density

We used tetracycline biomarking, augmented with genetic methods to estimate the size of an American black bear (Ursus americanus) population on an island in Southeast Alaska. We marked 132 and 189 bears that consumed remote, tetracycline-laced baits in 2 different years, respectively, and observed 39 marks in 692 bone samples subsequently collected from hunters. We genetically analyzed hair samples from bait sites to determine the sex of marked bears, facilitating derivation of sex-specific population estimates. We obtained harvest samples from beyond the study area to correct for emigration. We estimated a density of 155 independent bears/100 km², which is equivalent to the highest recorded for this species. This high density appears to be maintained by abundant, accessible natural food. Our population estimate (approx. 1,000 bears) could be used as a baseline and to set hunting quotas. The refined biomarking method for abundance estimation is a useful alternative where physical captures or DNA-based estimates are precluded by cost or logistics. © 2011 The Wildlife Society.     

Environmental conditions influence red grouse ornamentation at a population level

Theory suggests that condition‐dependent sexual displays should be more weakly expressed under adverse conditions than under more favourable ones. Here, we tested this hypothesis in wild red grouse Lagopus lagopus scoticus using a data set of nearly 1500 individuals from nine populations over 8 years, covering varying environmental conditions. We analysed whether male and female ornament expression (i.e. comb size) in a given site and year varied with various indices of environmental conditions: population density, Trichostrongylus tenuis nematode infection at the population level, and climate conditions [measured as winter North Atlantic oscillation (NAO) index]. We found that average comb size in males, but not in females, negatively correlated with population density, parasite infection levels, and winter NAO index. Furthermore, the coefficient of variation (CV) of comb size was higher in females than in males. CVs in both males and females were not clearly associated with the studied environmental variables. Our results support the idea that the expression of condition‐dependent sexual traits should be lower under more stressful environmental conditions, but only in males. We discuss the potential reasons behind the effect of environmental conditions on secondary sexual traits, and why these effects differ between sexes. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, ?? , ??–??.     

Growth and survivorship as proximate causes of sexual size dimorphism in peninsula dragon lizards Ctenophorus fionni

Males and females differ in body size in many animals, but the direction and extent of this sexual size dimorphism (SSD) varies widely. Males are larger than females in most lizards of the iguanian clade, which includes dragon lizards (Agamidae). I tested whether the male larger pattern of SSD in the peninsula dragon lizard, Ctenophorus fionni, is a result of sexual selection for large male size or relatively higher mortality among females. Data on growth and survivorship were collected from wild lizards during 1991–1994. The likelihood of differential predation between males and females was assessed by exposing pairs of male and female lizards to a predator in captivity, and by comparing the frequency of tail damage in wild‐caught males and females. Male and female C. fionni grew at the same rate, but males grew for longer than females and reached a larger asymptotic size (87 mm vs. 78 mm). Large males were under‐represented in the population because they suffered higher mortality than females. Predation may account for some of this male‐biased mortality. The male‐biased SSD in C. fionni resulted from differences in growth pattern between the sexes. The male‐biased SSD was not the result of proximate factors reducing female body size. Indeed SSD in this species remained male‐biased despite high mortality among large males. SSD in C. fionni is consistent with the ultimate explanation of sexual selection for large body size in males.     

Dietary adjustability of grizzly bears and American black bears in Yellowstone National Park

Grizzly bears (Ursus arctos) and American black bears (U. americanus) are sympatric in much of Yellowstone National Park. Three primary bear foods, cutthroat trout (Oncorhynchus clarki), whitebark pine (Pinus albicaulis) nuts, and elk (Cervus elaphus), have declined in recent years. Because park managers and the public are concerned about the impact created by reductions in these foods, we quantified bear diets to determine how bears living near Yellowstone Lake are adjusting. We estimated diets using: 1) stable isotope and mercury analyses of hair samples collected from captured bears and from hair collection sites established along cutthroat trout spawning streams and 2) visits to recent locations occupied by bears wearing Global Positioning System collars to identify signs of feeding behavior and to collect scats for macroscopic identification of residues. Approximately 45 ± 22% ( ± SD) of the assimilated nitrogen consumed by male grizzly bears, 38 ± 20% by female grizzly bears, and 23 ± 7% by male and female black bears came from animal matter. These assimilated dietary proportions for female grizzly bears were the same as 10 years earlier in the Lake area and 30 years earlier in the Greater Yellowstone Ecosystem. However, the proportion of meat in the assimilated diet of male grizzly bears decreased over both time frames. The estimated biomass of cutthroat trout consumed by grizzly bears and black bears declined 70% and 95%, respectively, in the decade between 1997–2000 and 2007–2009. Grizzly bears killed an elk calf every 4.3 ± 2.7 days and black bears every 8.0 ± 4.0 days during June. Elk accounted for 84% of all ungulates consumed by both bear species. Whitebark pine nuts continue to be a primary food source for both grizzly bears and black bears when abundant, but are replaced by false-truffles (Rhizopogon spp.) in the diets of female grizzly bears and black bears when nut crops are minimal. Thus, both grizzly bears and black bears continue to adjust to changing resources, with larger grizzly bears continuing to occupy a more carnivorous niche than the smaller, more herbivorous black bear. © 2012 The Wildlife Society.     

Population structure,demography, and dynamics of mountain baboons: An interim report

Counts of 61 baboon troops (Papio cynocephalus ursinus) at four localities in the Drakensberg mountains confirmed earlier reports of a small mean troop size. This troop size of 22.49 animals changed neither with latitude nor elevation. Data from two of the sites suggested that population density increases from south to north, while a working assumption of 2.5 animals/ km² allowed us to set the population size at 7,540 animals, living in 335 troops. Both the adult sex ratio of 2.07 females/male and the immature/ adult female ratio of 1.17 were unaffected by troop size. Repeated counts from nine known troops revealed that the population is at equilibrium. © 1995 Wiley-Liss, Inc.